Preface xix
P/N 85213-30, Manual revision: B
Note: The MCS+ device contains no user serviceable/repairable parts.
Caution: The MCS+ device must be operated in an environment compatible to
the requirements of the IEC 60601-1-2 Standard, Electromagnetic compatibility.
Mobile RF communication equipment not approved by Haemonetics and porta-
ble communication equipment can affect the MCS+ device. Any accessories and
cables not approved by Haemonetics used in conjunction with the device may
increase hazards and influence compatibility with EMC requirements. Therefore,
non-approved accessories and cables must not be used.
In addition, the MCS+ device and accessories must not be placed directly adja-
cent to, or top of other equipment, unless specifically approved by Haemonetics.
Caution: The MCS+ device must be operated in an environment compatible to
the requirements of IEC60601-1-1 Standard, Medical electrical equipment.
Any electrical equipment used inside or outside the “patient environment” (as de-
fined in the Standard), whether connected or not connected to the MCS+ device,
must provide a level of safety compliant with relevant IEC and ISO safety stan-
dards. Safe environmental conditions must be maintained for all devices inside
and outside of the patient environment.
When properly operated and maintained, the MCS+ device provides a level of
safety compliant with the IEC 60601-1-1 Standard, both inside and outside the
patient environment.
The operator is responsible for making sure that the final configuration of the
MCS+ device complies with IEC 60601-1-1 Standard, Medical electrical equip-
ment.
Note: Refer to the Postscript to the MCS+ Operation Manual (P/N 85270-30), for
information about Haemonetics approved devices, such as a printer or an exter-
nal network, that can be connected to the MCS+ device.
Note: The MCS+ device contains no user serviceable/repairable parts.
Caution: The MCS+ device must be operated in an environment compatible to
the requirements of the IEC 60601-1-2 Standard, Electromagnetic compatibility.
Mobile RF communication equipment not approved by Haemonetics and porta-
ble communication equipment can affect the MCS+ device. Any accessories and
cables not approved by Haemonetics used in conjunction with the device may
increase hazards and influence compatibility with EMC requirements. Therefore,
non-approved accessories and cables must not be used.
In addition, the MCS+ device and accessories must not be placed directly adja-
cent to, or top of other equipment, unless specifically approved by Haemonetics.
Caution: The MCS+ device must be operated in an environment compatible to
the requirements of IEC60601-1-1 Standard, Medical electrical equipment.
Any electrical equipment used inside or outside the “patient environment” (as de-
fined in the Standard), whether connected or not connected to the MCS+ device,
must provide a level of safety compliant with relevant IEC and ISO safety stan-
dards. Safe environmental conditions must be maintained for all devices inside
and outside of the patient environment.
When properly operated and maintained, the MCS+ device provides a level of
safety compliant with the IEC 60601-1-1 Standard, both inside and outside the
patient environment.
The operator is responsible for making sure that the final configuration of the
MCS+ device complies with IEC 60601-1-1 Standard, Medical electrical equip-
ment.
Note: Refer to the Postscript to the MCS+ Operation Manual (P/N 85270-30), for
information about Haemonetics approved devices, such as a printer or an exter-
nal network, that can be connected to the MCS+ device.
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